NEONATAL SALIVARY GENOMICS

• US 20110118125A1
• Filed: 05/01/2009
• Published: 05/19/2011
• Est. Priority Date: 05/03/2008
• Status: Abandoned Application

• Current Assignee: Tufts University
• Original Assignee: Tufts Medical Center Incorporated (Healthcare Realty Trust, Inc.), Tufts University
• Inventors: Maron, Jill, Bianchi, Diana, Slonim, Donna, Johnson, Kirby
• Application Number:
  US12/990,855
• Publication Number:
  US 20110118125A1
• Time in Patent Office: Days
• US Class Current: 506/4
• CPC Class Codes: C12Q 1/6883 for diseases caused by alterations of genetic material
• CPC Class Codes: C12Q 2600/158 Expression markers

Abstract

The present invention provides systems for assessing neonatal development and/or conditions by analyzing neonatal saliva RNA. Methods of identifying genes involved in neonatal development and/or conditions affecting neonates, are provided. Methods of determining a diagnosis of a neonate comprising detection of one or more differentially expressed genes are also provided.

Claims

1. A method for detecting or identifying genes involved in a condition or disease affecting neonates comprising steps of:

providing a test sample of saliva RNA obtained from a neonate suffering from or diagnosed with a condition;

subjecting the test sample of saliva RNA to an analysis, wherein the analysis comprises hybridizing the RNA to one or more oligonucleotide probes, such that one or more genes that are differentially regulated in the sample as compared to a control sample is/are identified, wherein the control sample comprises saliva RNA obtained from a neonate that is not suffering from or diagnosed with the condition; and

determining that the one or more differentially regulated genes are involved in the condition or disease.

2. The method of claim 1, wherein the condition is selected from the group consisting of necrotizing enterocolitis, respiratory distress syndrome, bronchopulmonary dysplasia, sepsis, and combinations thereof.

3. The method of claim 2, wherein the condition is necrotizing enterocolitis.

7. The method of claim 1 or 4, wherein the test sample of saliva RNA comprises a plurality of nucleic acid segments labeled with a detectable agent and wherein the step of identifying comprises:

providing a gene-expression array comprising a plurality of genetic probes, wherein each genetic probe is immobilized to a discrete spot on a substrate surface to form an array;

contacting the array with the test sample under conditions wherein the nucleic acid segments in the sample specifically hybridize to the genetic probes on the array;

determining the binding of individual nucleic acid segments of the test sample to individual genetic probes immobilized on the array to obtain a binding pattern; and

establishing, based on the binding pattern obtained, a gene expression pattern.

8. A method for determining a diagnosis of a neonate comprising steps of:

providing a sample of saliva RNA obtained from the neonate;

subjecting the test sample of saliva RNA to an analysis, wherein the analysis comprises hybridizing the RNA to one or more oligonucleotide probes, such that expression of at least one gene identified using the method of claim 1 or 4 is identified;

and determining, based on the detected expression of the at least one gene, a diagnosis of the neonate.

9. The method of claim 8, wherein the step of determining a diagnosis comprises determining neonatal developmental progress.

10. The method of claim 9, wherein determining neonatal developmental progress comprises making a determination with respect to a feeding capability of the neonate.

11. The method of claim 10, wherein the feeding capability is selected from the group consisting of readiness to feed, feeding tolerance, and combinations thereof.

12. The method of claim 11, wherein the step of determining a diagnosis comprises identifying a disease or condition affecting the neonate.

13. The method of claim 12, wherein the disease or condition is necrotizing enterocolitis.

14. The method of claim 8, wherein the at least one gene is upregulated during neonatal development.

15. The method of claim 14, wherein the at least one gene is selected from the group consisting of neuropeptide Y receptor Y1 (NPY1R);

leptin receptor (LEPR);

growth hormone secretagogue receptor (GHSR);

prostaglandin E receptor 3 (subtype EP3) (PTGER

     3);

hypocretin (orexin) receptor 2 (HCRTR2);

galanin receptor 3 (GALR3);

lactalbumin alpha (LALBA);

glucagon (GCG);

melanin-concentrating hormone receptor 1 (MCHR1);

prostaglandin E receptor 3 (PTGER3);

cholecytokinin A receptor (CCKAR);

odorant binding protein 2B (OBP2B);

transient receptor potential cation channel, subfamily V, member 1 (TRPV1);

taste receptor, type 2, member 1 (TAS2R1);

surfactant protein B (SFTPB);

cystic fibrosis transmembrane conductance regulator (CFTR);

fibroblast growth factors (FGF) 1, 2, 7, 10, 18;

fibroblast growth receptor 2 (FGFR2); and

combinations thereof.

16. The method of claim 8, wherein the at least one gene is downregulated during neonatal development.

17. The method of claim 16, wherein the at least one gene is selected from the group consisting of carcinoembryonic antigen-related cell adhesion molecule 1 (biliary glycoprotein) (CEACAM1);

V-raf murine sarcoma viral oncogene homolog B1 (BRAF);

amino-terminal enhancer of split (AES);

E1A binding protein p300 (EP300);

Fas (TNF receptor superfamily member

     6) (FAS);

Fas (TNFRSF6)-associated via death domain (FADD);

cyclin-dependent kinase inhibitor 2A (melanoma, p16, inhibits CDK4) (CDKN2A);

glycogen synthase kinase 3 Beta (GSK3B);

protein kinase, cAMP-dependent, regulatory, type 1, alpha (tissue specific extinguisher

     1) (PRKAR1A);

signal transducer and activator of transcription 5B (STAT5B);

aryl hydrocarbon receptor nuclear translocator (ARNT);

insulin receptor (INSR); and

combinations thereof.

18. The method of claim 8, further comprising detecting at least one gene selected from the group consisting of nuclear factor kappa B (NFκ

B), I kappa B-alpha (Iκ

B-α

), toll-like receptor 4 (TLR4), platelet activating factor (PAF), platelet activating factor acetylhydrolase (PAF-AH), interleukin 8 (IL-8), epidermal growth factor (EGF), interleukin 10 (IL-10), endothelial 1 (ET-1), and combinations thereof.

4. A method for detecting or identifying genes involved in neonatal development comprising steps of:

providing a test sample of saliva RNA obtained from a neonate;

subjecting the test sample of saliva RNA to an analysis, wherein the analysis comprises hybridizing the RNA to one or more oligonucleotide probes, such that one or more genes that are differentially regulated in the sample as compared to a control sample is/are detected or identified, wherein the control sample comprises saliva RNA obtained from a neonate at a developmental stage different than the neonate from which the test sample of saliva RNA sample was obtained; and

determining that the one or more differentially regulated genes are involved in neonatal development.

5. The method of claim 4, wherein the developmental stage is assessed with respect to the neonate'"'"'s feeding capability.

6. The method of claim 4, wherein the feeding capability is selected from the group consisting of readiness to feed, feeding tolerance, and combinations thereof.